Results 311 to 320 of about 2,371,477 (389)

Differences in activity and stability drive transposable element variation in tropical and temperate maize. [PDF]

open access: yesGenome Res
Ou S   +11 more
europepmc   +1 more source

The spatial distribution of a hummingbird‐pollinated plant is not strongly influenced by hummingbird abundance

open access: yesAmerican Journal of Botany, EarlyView.
Abstract Premise Many angiosperms have evolved specialized systems that promote pollination by specific taxa. Therefore, plant distributions may be limited by the local abundance of their specialist pollinators. In eastern North America, Lobelia cardinalis is thought to be pollinated solely by Archilochus colubris, the only hummingbird species found in
Matthew L. Coffey, Andrew M. Simons
wiley   +1 more source

Cell-Specific Transposable Element and Gene Expression Analysis Across Systemic Lupus Erythematosus Phenotypes. [PDF]

open access: yesACR Open Rheumatol
Cutts Z   +12 more
europepmc   +1 more source

A transposable element prevents severe hemophilia B and provides insights into the evolution of new- and old world primates. [PDF]

open access: yesPLoS One
Kopp J   +9 more
europepmc   +1 more source

Nanopore Sequencing Solves an Elusive Case of Sotos Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Sotos syndrome is a rare genetic disorder characterized by distinctive facial features, including a broad and prominent forehead, dolichocephaly, and learning disabilities ranging from mild to severe intellectual impairment. Affected individuals often show overgrowth in height and head circumference over two standard deviations.
Pasquale Di Letto   +52 more
wiley   +1 more source

Phenotypic Characterization of Seven Pediatric Patients Diagnosed With KAT6B‐Related Disorders: Case Series and Review of the Literature

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Genitopatellar syndrome (GPS) and Say‐Barber‐Biesecker‐Young‐Simpson Syndrome (SBBYSS) are clinically distinct neurodevelopmental disorders caused by monoallelic pathogenic variants in KAT6B. In some cases, GPS and SBBYSS features can overlap, determining an intermediate phenotype.
Vittorio Maglione   +12 more
wiley   +1 more source

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